MAQUET : FDA labels IABP recall for Getinge's Maquet, Datascope as Class I

The FDA today labeled a select recall of Getinge's (PINK:GETI B) Datascope and Maquet Cardiosave hybrid intra-aortic balloon pumps over issues related to fluid seepage and corrosion as Class I. A Class I recall is the federal watchdog's most serious class of recall, indicating the potential for serious injury or death. The Cardiosave hybrid intra-aortic balloon pump is designed [...]The post FDA labels IABP recall for Getinge's Maquet, Datascope as Class I appeared first on MassDevice.